CAR-T Cell Therapy

Cutting-Edge, Personalised Immunotherapy for Blood Cancers

Introduction

Chimeric Antigen Receptor T-Cell Therapy—commonly known as CAR-T cell therapy—is one of the most advanced, personalised forms of cancer treatment available today. Unlike chemotherapy, targeted therapy, or standard immunotherapy, CAR-T uses the patient’s own immune cells, genetically engineers them to recognise cancer, and re-infuses them to launch a focused attack on malignant cells.

This approach has revolutionised outcomes in several blood cancers, especially in patients whose disease has relapsed multiple times or become resistant to conventional treatments. CAR-T therapy represents the frontier of precision oncology and offers new hope when traditional treatment options have been exhausted.

At our clinic, CAR-T therapy is offered through specialised referral networks and accredited centres, ensuring stringent selection, rigorous monitoring, and comprehensive pre- and post-treatment support.

1. What Is CAR-T Cell Therapy?

CAR-T therapy is a highly individualised treatment that involves modifying a patient’s own T-cells (a type of white blood cell) to attack cancer. The treatment involves:

CAR-T therapy gives the immune system a “new set of instructions” to fight cancer more effectively.

2. How CAR-T Cells Work

Cancer cells often avoid detection by hiding their antigens or suppressing the immune system. CAR-T therapy bypasses these escape mechanisms.

Mechanism of Action

This makes CAR-T cell therapy fundamentally different from most traditional treatments.

3. Cancers Treated with CAR-T Therapy

Currently, CAR-T therapy is primarily used in haematological malignancies.

Approved Indications Include:

Research is ongoing for applications in:

However, these are still investigational.

4. Steps in CAR-T Therapy

The CAR-T process typically takes several weeks and involves multiple stages.

1. Patient Evaluation

A multidisciplinary team assesses:

Not all patients are suitable candidates, especially those with severe organ dysfunction or rapidly progressing disease.

2. T-Cell Collection (Leukapheresis)

Blood is passed through a machine that isolates T-cells, while the rest of the blood returns to the body.

3. Genetic Engineering

In a controlled laboratory facility:

4. Cell Expansion

Millions to billions of CAR-T cells are grown in the lab over 2–3 weeks.

5. Lymphodepleting Chemotherapy

Before infusion, patients receive low-dose chemotherapy to:

This is not high-intensity chemotherapy.

6. CAR-T Cell Infusion

CAR-T cells are infused in a single, controlled setting.

This is similar to a blood transfusion.

7. Monitoring and Support

Patients are monitored closely for side effects, usually requiring hospital admission for 7–14 days.

5. Benefits of CAR-T Therapy

1. High Response Rates in Refractory Disease

Many patients who have failed multiple lines of treatment can achieve:

2. Potential for Long-Term Cure

CAR-T cells can persist and continue protecting the patient.

3. Personalised Treatment

Because CAR-T is made from the patient’s own cells, it is tailored uniquely for each individual.

4. Single Administration

Unlike chemotherapy cycles, CAR-T therapy is typically a one-time infusion.

5. Deeper Responses

CAR-T cells can reach cancer cells in locations where chemotherapy may be ineffective.

6. Potential Risks and Side Effects

CAR-T therapy is powerful, but its immune activation can lead to significant side effects that require expert management.

1. Cytokine Release Syndrome (CRS)

The most common side effect.

Symptoms Include:

Management includes:

2. Immune Effector Cell–Associated Neurotoxicity Syndrome (ICANS)

A unique neurological toxicity.

Symptoms:

3. Infections

Due to immune suppression.

4. Low Blood Counts

Temporary but common.

5. Tumour Lysis Syndrome

Rapid cancer cell death leading to electrolyte imbalances.

Our Safety Protocols Include:

CAR-T therapy requires specialist infrastructure; we coordinate care with accredited centres to ensure safety.

7. Follow-Up and Recovery After CAR-T Therapy

Recovery continues for weeks to months.

Short-Term Follow-Up

Long-Term Follow-Up

Patients often continue prophylactic medications to prevent infections.

8. Who Is Not Eligible for CAR-T Therapy?

CAR-T may not be suitable for patients with:

Our clinical team conducts a detailed evaluation before proceeding.

9. CAR-T vs Other Treatments

Feature CAR-T Therapy Chemotherapy Immunotherapy
Personalisation EHighest Moderate Biomarker-dependent
Mechanism Engineered immune cells Kills dividing cells Activates immune system
Administration One-time infusion Multiple cycles Regular infusions
Common Use Refractory blood cancers Most cancers Many solid tumours
Durability Potentially long-term Variable Long-term in responders

CAR-T is not a replacement for chemotherapy or immunotherapy but rather a specialised therapy for selected patients.

10. Our Clinic’s Role in CAR-T Therapy

We provide a complete, structured pathway for patients requiring CAR-T:

1. Patient Evaluation and Selection

Detailed assessment by our haematology and medical oncology experts.

2. Pre-CAR-T Preparation

3. Seamless Referral and Monitoring

We collaborate with accredited CAR-T treatment centres and manage:

4. Psychosocial, Nutritional, and Family Support

CAR-T therapy is emotionally demanding. We support patients and caregivers throughout the process.

5. Survivorship Planning

Long-term monitoring and holistic care beyond remission.

Conclusion

CAR-T cell therapy represents a landmark shift in cancer treatment. For selected patients with relapsed or refractory blood cancers, it offers deep, durable responses and the possibility of long-term remission—even after multiple previous treatment failures.

Our clinic ensures that every patient considered for CAR-T therapy receives expert evaluation, comprehensive counselling, and coordinated, high-quality care throughout the entire treatment journey. With a commitment to Cure, Precision, and Compassion, we guide patients through every stage of this advanced, life-changing therapy.